This paper evaluates the adsorption capacity of chemically sugarcane bagasses with sodium hydroxide(SHS),citric acid(CAS),tartaric acid(TAS)and unmodified sugarcane bagasse(SB)for cadmium adsorption in water environme...This paper evaluates the adsorption capacity of chemically sugarcane bagasses with sodium hydroxide(SHS),citric acid(CAS),tartaric acid(TAS)and unmodified sugarcane bagasse(SB)for cadmium adsorption in water environment.The results prove adsorption capacity for Cd(II)increases after chemical modification and the adsorption fits perfectly with the Langmuir isotherm.CAS had the highest maximum adsorption capacity of 45.45 mg/g followed by TAS with 38.46 mg/g and SHS with 29.41 at optimum pH 5.0 and 120 minutes equilibrium time while 1 g SB removed 18.8 mg Cd(II)in the same conditions.The kinetics study of the process followed a pseudo-secondorder rate expression,that indicated a strong interaction between the biosorbents and adsorbate.The sugarcane bagasse and modified sugarcane bagasse were characterized by scanning electron microscopy(SEM)and Fourier transform infrared spectroscopy(FTIR)analysis.The chemical modification was confirmed by the presence of carboxyl and esters groups created at 1,738 cm-1.The estimation of acid groups in modified materials shows the enhancement of this group after modification.On the other hand,desorption studies showed the high leaching of cadmium ion from the biosorbent leading to the efficient reutilization of materials.展开更多
Proton exchange membrane(PEM)water electrolysis represents a promising technology for green hydrogen production,but its widespread deployment is greatly hindered by the indispensable usage of platinum group metal cata...Proton exchange membrane(PEM)water electrolysis represents a promising technology for green hydrogen production,but its widespread deployment is greatly hindered by the indispensable usage of platinum group metal catalysts,especially iridium(Ir)based materials for the energy-demanding oxygen evolution reaction(OER).Herein,we report a new sequential precipitation approach to the synthesis of mixed Ir-nickel(Ni)oxy-hydroxide supported on antimony-doped tin oxide(ATO)nanoparticles(IrNiyO_(x)/ATO,20 wt.%(Ir+Ni),y=0,1,2,and 3),aiming to reduce the utilisation of scarce and precious Ir while maintaining its good acidic OER performance.When tested in strongly acidic electrolyte(0.1 M HClO_(4)),the optimised IrNi1Ox/ATO shows a mass activity of 1.0 mAµgIr^(−1) and a large turnover frequency of 123 s^(−1) at an overpotential of 350 mV,as well as a comparatively small Tafel slope of 50 mV dec^(−1),better than the IrOx/ATO control,particularly with a markedly reduced Ir loading of only 19.7µgIr cm^(−2).Importantly,IrNi1O_(x)/ATO also exhibits substantially better catalytic stability than other reference catalysts,able to continuously catalyse acidic OER at 10 mA cm^(−2) for 15 h without obvious degradation.Our in-situ synchrotron-based x-ray absorption spectroscopy confirmed that the Ir^(3+)/Ir^(4+)species are the active sites for the acidic OER.Furthermore,the performance of IrNi1Ox/ATO was also preliminarily evaluated in a membrane electrode assembly,which shows better activity and stability than other reference catalysts.The IrNi1Ox/ATO reported in this work is a promising alternative to commercial IrO_(2) based catalysts for PEM electrolysis.展开更多
文摘This paper evaluates the adsorption capacity of chemically sugarcane bagasses with sodium hydroxide(SHS),citric acid(CAS),tartaric acid(TAS)and unmodified sugarcane bagasse(SB)for cadmium adsorption in water environment.The results prove adsorption capacity for Cd(II)increases after chemical modification and the adsorption fits perfectly with the Langmuir isotherm.CAS had the highest maximum adsorption capacity of 45.45 mg/g followed by TAS with 38.46 mg/g and SHS with 29.41 at optimum pH 5.0 and 120 minutes equilibrium time while 1 g SB removed 18.8 mg Cd(II)in the same conditions.The kinetics study of the process followed a pseudo-secondorder rate expression,that indicated a strong interaction between the biosorbents and adsorbate.The sugarcane bagasse and modified sugarcane bagasse were characterized by scanning electron microscopy(SEM)and Fourier transform infrared spectroscopy(FTIR)analysis.The chemical modification was confirmed by the presence of carboxyl and esters groups created at 1,738 cm-1.The estimation of acid groups in modified materials shows the enhancement of this group after modification.On the other hand,desorption studies showed the high leaching of cadmium ion from the biosorbent leading to the efficient reutilization of materials.
基金supported by the National Innovation Agency of Portugal through the project Baterias 2030(Grant No.POCI-01-0247-FEDER-046109)J R E would like to acknowledge the Fundación General CSIC’s ComFuturo programme which has received funding from the European Union’s Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie grant agreement No.101034263+2 种基金The authors appreciate Dr Laura Simonelli and Dr Vlad Martin Diaconescu for their assistance in XAS measurements at the beamline BL22-CLÆSS,ALBA synchrotron(experiment AV-2022025706)R M is grateful to the Portuguese Foundation for Science and Technology(FCT)for the doctoral grant(Grant No.2021.06496.BD)R M and A M are grateful for the financial support from:LA/P/0045/2020,UIDB/00511/2020 and UIDP/00511/2020,funded by the national funds through FCT/MCTES(PIDDAC)。
文摘Proton exchange membrane(PEM)water electrolysis represents a promising technology for green hydrogen production,but its widespread deployment is greatly hindered by the indispensable usage of platinum group metal catalysts,especially iridium(Ir)based materials for the energy-demanding oxygen evolution reaction(OER).Herein,we report a new sequential precipitation approach to the synthesis of mixed Ir-nickel(Ni)oxy-hydroxide supported on antimony-doped tin oxide(ATO)nanoparticles(IrNiyO_(x)/ATO,20 wt.%(Ir+Ni),y=0,1,2,and 3),aiming to reduce the utilisation of scarce and precious Ir while maintaining its good acidic OER performance.When tested in strongly acidic electrolyte(0.1 M HClO_(4)),the optimised IrNi1Ox/ATO shows a mass activity of 1.0 mAµgIr^(−1) and a large turnover frequency of 123 s^(−1) at an overpotential of 350 mV,as well as a comparatively small Tafel slope of 50 mV dec^(−1),better than the IrOx/ATO control,particularly with a markedly reduced Ir loading of only 19.7µgIr cm^(−2).Importantly,IrNi1O_(x)/ATO also exhibits substantially better catalytic stability than other reference catalysts,able to continuously catalyse acidic OER at 10 mA cm^(−2) for 15 h without obvious degradation.Our in-situ synchrotron-based x-ray absorption spectroscopy confirmed that the Ir^(3+)/Ir^(4+)species are the active sites for the acidic OER.Furthermore,the performance of IrNi1Ox/ATO was also preliminarily evaluated in a membrane electrode assembly,which shows better activity and stability than other reference catalysts.The IrNi1Ox/ATO reported in this work is a promising alternative to commercial IrO_(2) based catalysts for PEM electrolysis.
